Rhabdomyosarcoma of Orbit: A Rare Case Report and Review.

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dc.contributor.authorNagarkar, Rajnish
dc.contributor.authorRoy, Shirsendu
dc.contributor.authorAkheel, Mohammad
dc.contributor.authorPalwe, Vijay
dc.contributor.authorKulkarni, Nayana
dc.date.accessioned2015-07-08T12:18:35Z
dc.date.available2015-07-08T12:18:35Z
dc.date.issued2014-10
dc.description.abstractRhabdomyosarcoma (RMS) is a highly fulminant, mesenchymal malignant tumor and is considered to be one among life-threatening disease in the present decades. It is considered to be most common malignant neoplasm of the head and neck region with 10% of cases occurring in orbit. Th ough it is common in sixth and seventh decades, it can also occur in early childhood. In this article, we present a rare case of 9-yearold boy who was diagnosed with histopathologically proven RMS of orbit who had undergone a salvage left orbital exenteration following a chemotherapy. Th e main aim of this article is also to provide an overview of RMS of orbit, clinical features, investigations required, staging and various treatment modalities.en_US
dc.identifier.citationNagarkar Rajnish, Roy Shirsendu, Akheel Mohammad, Palwe Vijay, Kulkarni Nayana. Rhabdomyosarcoma of Orbit: A Rare Case Report and Review. IJSS Case Reports & Reviews. 2014 Oct; 1(5): 6-10.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/159341
dc.language.isoenen_US
dc.source.urihttps://www.ijsscr.com/sites/default/files/articles/IJSS-1-6.xmlen_US
dc.subjectMalignant tumoren_US
dc.subjectNeoplasmen_US
dc.subjectRhabdomyosarcomaen_US
dc.subject.meshChild
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshOrbit Neoplasms --diagnosis
dc.subject.meshOrbit Neoplasms--pathology
dc.subject.meshOrbit Neoplasms --surgery
dc.subject.meshReview Literature as Topic
dc.subject.meshRhabdomyosarcoma --diagnosis
dc.subject.meshRhabdomyosarcoma -drug therapy
dc.subject.meshRhabdomyosarcoma --pathology
dc.titleRhabdomyosarcoma of Orbit: A Rare Case Report and Review.en_US
dc.typeArticleen_US
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